Clinical trial Recruiting at 1 site Interventional Ages 18 to 45

Optimized pumping protocols to see if milk production improves in new mothers

Official title: Facilitating Lactation Through Optimized Workflows - Evaluating the Efficiency of Pumping Protocols and Cellular Mechanisms of Milk Production

Run by University of Rochester · NCT07260968 · Data updated 2026-11-12

This study tests two breast pumping schedules to see if they help lactating parents with low milk supply.

Quick facts

Study typeInterventional
Ages18 Years to 45 Years
SexAll
Enrollment225 (estimated)
SponsorUniversity of Rochester
Academic / other
Locations1 site (Rochester, New York)
StatusRecruiting
StartedMay 7, 2026
Main results expectedDecember 20, 2027
Study endsSeptember 30, 2028
Registry record updatedJune 4, 2026
Trial IDNCT07260968 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Lactating parents of singleton, term infants under 3 months who plan to breastfeed and currently breastfeed at least three times daily.

Probably not a fit

Individuals whose milk production is not responsive to pumping protocol changes or who have contraindications to breastfeeding may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study compares two pumping frequency protocols to determine their effect on milk production in lactating individuals with primary low milk supply. The study also explores related molecular, hormonal, and inflammatory factors that may influence milk output. Participants are English-speaking, have singleton term infants under 3 months, and currently breastfeed at least three times daily. The investigation is conducted at URMC with collaboration from Cornell University, led by the University of Rochester, and requires access to electricity and a smartphone. Outcomes include changes in milk production and insights into biological mechanisms underlying lactation.

Why it matters

Potential benefit: Participants may experience increased milk production with the optimized pumping approach if the protocol is effective.

How similar studies have gone: Prior research on pumping regimens has shown variable results; this study adds mechanistic insights but the approach is relatively novel for this specific population.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* English-speaking
* Lactating parents of singleton, term infants less than 3 months of age
* Intend to breastfeed and are breastfeeding (at the breast) at least 3 times per day

Exclusion criteria:

* Twins and other multiples
* Contraindications to or unable to breastfeed
* Major congenital anomaly or unexpected surgery
* Elevated maternal depression
* Low milk transfer
* No electricity or smartphone access

Where it's running

  • URMC Breastfeeding & Lactation Clinic
    Rochester, New York, United States
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.